Canonical Allele Identifier: CA380690823

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381987T>C (hg19) ; chr11:g.57614514T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614514T>C , CM000673.2:g.57614514T>C	GRCh38
NC_000011.9:g.57381987T>C , CM000673.1:g.57381987T>C	GRCh37
NC_000011.8:g.57138563T>C	NCBI36
NG_009625.1:g.21961T>C , LRG_105:g.21961T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1436T>C MANE Select	ENSP00000278407.4:p.Phe479Ser
ENST00000528996.2:c.*333T>C	ENSP00000431226.2:n.*333T>C
ENST00000531605.2:c.*1212T>C	ENSP00000503752.1:n.*1212T>C
ENST00000619430.2:c.1232T>C	ENSP00000478572.2:p.Phe411Ser
ENST00000676670.1:c.1436T>C	ENSP00000504807.1:p.Phe479Ser
ENST00000676741.1:n.2518T>C
ENST00000677624.1:c.*856T>C	ENSP00000503979.1:n.*856T>C
ENST00000677625.1:c.1382T>C	ENSP00000502857.1:p.Phe461Ser
ENST00000677856.1:n.1689T>C
ENST00000677915.1:c.*333T>C	ENSP00000503118.1:n.*333T>C
ENST00000678533.1:c.*990T>C	ENSP00000503873.1:n.*990T>C
ENST00000678592.1:c.*376T>C	ENSP00000504424.1:n.*376T>C
ENST00000278407.8:c.1436T>C	ENSP00000278407.4:p.Phe479Ser
ENST00000340687.10:c.1325T>C	ENSP00000341861.6:p.Phe442Ser
ENST00000378323.8:c.1451T>C	ENSP00000367574.4:p.Phe484Ser
ENST00000378324.6:c.1280T>C	ENSP00000367575.2:p.Phe427Ser
ENST00000403558.1:c.1565T>C	ENSP00000384420.1:p.Phe522Ser
ENST00000528996.1:c.637T>C	ENSP00000431226.1:n.637T>C
ENST00000530113.1:n.893T>C
ENST00000531133.5:c.937T>C	ENSP00000435431.1:n.937T>C
ENST00000531797.5:c.*461T>C	ENSP00000432554.1:n.*461T>C
ENST00000619430.1:c.567T>C	ENSP00000478572.1:n.567T>C
NM_000062.2:c.1436T>C , LRG_105t1:c.1436T>C	NP_000053.2:p.Phe479Ser
NM_001032295.1:c.1436T>C	NP_001027466.1:p.Phe479Ser
NM_000062.3:c.1436T>C MANE Select	NP_000053.2:p.Phe479Ser
NM_001032295.2:c.1436T>C	NP_001027466.1:p.Phe479Ser